A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7669n100



Internal ID20159285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69413542..69434676hg38UCSC Ensembl
chr9:72028458..72049592hg19UCSC Ensembl
chr9:71218278..71239412hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3821135
hg1921135
hg1821135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049763, nsv1047666
Samples
Known GenesAPBA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7669n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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